A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113288



Internal ID21296554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11913186..11918645hg38UCSC Ensembl
Innerchr16:12007043..12012502hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg385460
hg195460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv424n145
Supporting Variantsnssv14096483
Samplessample308
Known GenesGSPT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113288
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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